NP-MRD: Showing NP-Card for Laxichalcone (NP0054795)

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Record Information

Version

2.0

Created at

2022-04-28 01:02:02 UTC

Updated at

2022-04-28 01:02:02 UTC

NP-MRD ID

NP0054795

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Laxichalcone

Description

Laxichalcone belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, laxichalcone is considered to be a flavonoid. Laxichalcone is found in Derris laxiflora and Derris laxifolia. Laxichalcone was first documented in 2016 (PMID: 26791751). Based on a literature review very few articles have been published on Laxichalcone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282203022D          

 30 33  0  0  0  0            999 V2000
    5.2520   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429    0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429    0.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 13 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -4.9273    3.1665   -0.1969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1971    2.2997    0.8498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2058    2.0911    1.9836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0593    3.1026    1.2985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8153    2.6826    1.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5151    1.3920    0.5839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2114    0.8918    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7856    1.6876    0.8635 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0811   -0.3243   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3677   -0.9146   -0.3312 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2955   -2.1331   -0.9116 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7170   -0.5902   -0.0959 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3987    0.3791    0.4037 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8684    0.3753    0.4912 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4549    1.5068    1.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8009    1.6463    1.2095 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6135    0.6240    0.7756 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0017    0.7046    0.8980 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0713   -0.5062    0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6751   -0.6273    0.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0661   -1.0577   -0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3439   -0.6008   -0.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5786    0.6301    0.1591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8578    1.0952    0.3012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4579   -1.4321   -0.8692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -2.6131   -1.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9036   -3.1515   -1.5875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6044   -3.5069   -3.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8425   -4.4352   -0.7499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8948   -2.2984   -1.1229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3230    3.0322   -1.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9738    2.8488   -0.3140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8230    4.2416    0.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1962    1.9781    1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2566    2.9741    2.6219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9950    1.1753    2.5438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2160    4.0990    1.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9924    3.3016    1.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136    2.5772    1.2857 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4558   -1.4234   -0.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985    1.2324    0.7767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8527    2.3516    1.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2800    2.5150    1.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5210    1.1075    0.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7259   -1.3005   -0.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3012   -1.5282   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4769   -1.0489   -0.7500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1440   -3.1581   -1.7268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7448   -2.6548   -3.6910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5143   -3.7860   -3.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1930   -4.3919   -3.2770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9588   -4.1976    0.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6030   -5.1369   -1.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8362   -4.8917   -0.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 24  1  0
 24 23  1  0
 23 22  2  0
 22 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 27 30  1  0
 30 21  1  0
 21  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
  9  7  1  0
  7  8  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  6 23  1  0
 21 22  1  0
 20 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
 25 47  1  0
 26 48  1  0
 28 49  1  0
 28 50  1  0
 28 51  1  0
 29 52  1  0
 29 53  1  0
 29 54  1  0
 12 40  1  0
 13 41  1  0
 15 42  1  0
 16 43  1  0
 18 44  1  0
 19 45  1  0
 20 46  1  0
  8 39  1  0
  5 38  1  0
  4 37  1  0
M  END


  Mrv1652304282203022D          

 30 33  0  0  0  0            999 V2000
    5.2520   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429    0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429    0.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 13 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054795

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=C3C=CC(C)(C)OC3=C(C(=O)\C=C\C3=CC=C(O)C=C3)C(O)=C2C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O5/c1-24(2)13-11-17-21(28)20(19(27)10-7-15-5-8-16(26)9-6-15)23-18(22(17)29-24)12-14-25(3,4)30-23/h5-14,26,28H,1-4H3/b10-7+

> <INCHI_KEY>
OYKNIXGSTSXINU-JXMROGBWSA-N

> <FORMULA>
C25H24O5

> <MOLECULAR_WEIGHT>
404.462

> <EXACT_MASS>
404.162373873

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
44.9709011665446

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-1-{5-hydroxy-2,2,8,8-tetramethyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-3-(4-hydroxyphenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
5.734441469666667

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.043256603290574

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.305676910429013

> <JCHEM_PKA_STRONGEST_BASIC>
-4.657554847391737

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
119.62560000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.29e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-1-{5-hydroxy-2,2,8,8-tetramethylpyrano[2,3-f]chromen-6-yl}-3-(4-hydroxyphenyl)prop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.804  -5.898   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.034  -4.565   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.804  -3.231   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.344  -3.231   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.114  -4.565   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.344  -5.898   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.654  -4.565   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.494  -4.565   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.724  -3.231   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -3.231   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.414  -4.565   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.104   2.104   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.742   2.920   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.510   3.643   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.724  -0.564   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.853   1.493   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.853   0.047   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5                                                            
CONECT    8    2    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14   28                                                  
CONECT   14   13   15   25                                                  
CONECT   15   14   16   22                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   12   18                                                  
CONECT   18   17                                                            
CONECT   19   16   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21   15                                                       
CONECT   23   21                                                            
CONECT   24   21                                                            
CONECT   25   14   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27   13                                                       
CONECT   29   27                                                            
CONECT   30   27                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₅

Average Mass

404.4620 Da

Monoisotopic Mass

404.16237 Da

IUPAC Name

(2E)-1-{5-hydroxy-2,2,8,8-tetramethyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-3-(4-hydroxyphenyl)prop-2-en-1-one

Traditional Name

(2E)-1-{5-hydroxy-2,2,8,8-tetramethylpyrano[2,3-f]chromen-6-yl}-3-(4-hydroxyphenyl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=C3C=CC(C)(C)OC3=C(C(=O)\C=C\C3=CC=C(O)C=C3)C(O)=C2C=C1

InChI Identifier

InChI=1S/C25H24O5/c1-24(2)13-11-17-21(28)20(19(27)10-7-15-5-8-16(26)9-6-15)23-18(22(17)29-24)12-14-25(3,4)30-23/h5-14,26,28H,1-4H3/b10-7+

InChI Key

OYKNIXGSTSXINU-JXMROGBWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Derris laxiflora	LOTUS Database	35616633
Derris laxifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxychalcones

Alternative Parents

Substituents

2'-hydroxychalcone
Pyranochromene
Cinnamic acid or derivatives
Hydroxycinnamic acid or derivatives
2,2-dimethyl-1-benzopyran
Benzopyran
1-benzopyran
Styrene
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Acryloyl-group
Enone
Vinylogous acid
Alpha,beta-unsaturated ketone
Ketone
Organoheterocyclic compound
Ether
Oxacycle
Aldehyde
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120260 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.9	ALOGPS
logP	5.73	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	7.31	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	119.63 m³·mol⁻¹	ChemAxon
Polarizability	44.97 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00007103

Chemspider ID

9677112

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11502310

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang LB, Lei C, Gao LX, Li JY, Li J, Hou AJ: Isoprenylated Flavonoids with PTP1B Inhibition from Macaranga denticulata. Nat Prod Bioprospect. 2016 Feb;6(1):25-30. doi: 10.1007/s13659-015-0082-2. Epub 2016 Jan 20. [PubMed:26791751 ]

Showing NP-Card for Laxichalcone (NP0054795)

MOL for NP0054795 (Laxichalcone)

3D MOL for NP0054795 (Laxichalcone)

3D SDF for NP0054795 (Laxichalcone)

3D-SDF for NP0054795 (Laxichalcone)

PDB for NP0054795 (Laxichalcone)

3D PDB for NP0054795 (Laxichalcone)

SMILES for NP0054795 (Laxichalcone)

INCHI for NP0054795 (Laxichalcone)

Structure for NP0054795 (Laxichalcone)

3D Structure for NP0054795 (Laxichalcone)